HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264630Generated: November 1, 2026
Triethylamine → 1-[[3-[[2,2-Dicyano-1-[(2-methyl-5-benzofuranyl)amino]ethenyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl]acetyl]pyrrolidine
https://huagongshe.com/reaction/1264630
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-5-benzofuranamine | HCID 3157484 | — |
| Reactant | 1-[(3-amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl)acetyl]pyrrolidine | HCID 18612553 | — |
| Reactant | 2-((Methylthio)methylene)malononitrile | HCID 18979789 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[[3-[[2,2-Dicyano-1-[(2-methyl-5-benzofuranyl)amino]ethenyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl]acetyl]pyrrolidine | HCID 18612617 | 3% |
Reaction Steps
Preparation of title compound. A solution of 2-methyl-5-benzofuranamine (0.24 mmol), 1,1-bis(methylthio-2,2-dicyanoethylene (34 mg, 0.20 mmol) and triethylamine (0.035 mL, 0.25 mmol) in ethanol (0.35 mL) was stirred at 80° C. for 4 h. To the mixture was added 1-[(3-amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl)acetyl]pyrrolidine (70 mg, 0.24 mmol) and the resulting reaction was stirred at 80° C. overnight. The reaction mixture was purified by column chromatography (silica, 5% methanol/ethyl acetate) to afford the title compound (3 mg, 3% yield): MS (ESI, pos. ion spectrum) m/z 509; HPLC (method A) tR 3.80 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544981B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-0ae0cd8413b64588ae4897cb0b3a898c |
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| Source note | uspto-grants-2003_04 |
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